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PMID: 7826947 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Human Fas ligand: gene structure, chromosomal location and species specificity.

International immunology ·Vol. 6 ·No. 10 ·1994-10-00 ·Pages 1567-74

Takahashi T, Tanaka M, Inazawa J, Abe T, Suda T, Nagata S

Abstract

Fas ligand (FasL) is a 40 kDa type II membrane protein belonging to the tumor necrosis factor family, which induces apoptosis by binding to its receptor, Fas. In this report, we isolated the chromosomal gene for human FasL. The human FasL gene consists of approximately 8.0 kb and is split into four exons. The human FasL gene was mapped on chromosome 1q23 by in situ hybridization against human metaphase chromosomes. Human FasL cDNA was isolated by the reverse polymerase chain reaction of mRNA prepared from human activated peripheral blood lymphocytes. Human FasL is a type II membrane protein consisting of 281 amino acids with a calculated M(r) of 31,759. It has an identity of 76.9% at the amino acid sequence level with mouse FasL. Both human and mouse recombinant FasL expressed in COS induced apoptosis in the cells expressing either human Fas or mouse Fas, indicating that FasL fully cross-reacts between human and mouse. A comparison of human and mouse FasL chromosomal genes indicated that a approximately 300 bp sequence upstream of the ATG initiation codon is highly conserved between them. Several transcription cis-regulatory elements such as SP-1, NF-kappa B and IRF-1 were recognized in this region.

Related Genes
MeSH Terms
Adult Amino Acid Sequence Base Sequence Chromosome Mapping Chromosomes, Human, Pair 1 Cloning, Molecular/methods Fas Ligand Protein Genomic Library Humans In Situ Hybridization, Fluorescence Membrane Glycoproteins/chemistry,genetics Molecular Sequence Data Polymerase Chain Reaction Sequence Homology, Amino Acid Species Specificity
Chemicals
FASLG protein, human Fas Ligand Protein Fasl protein, mouse Membrane Glycoproteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Takahashi T
Osaka Bioscience Institute, Japan.
Tanaka M
Inazawa J
Abe T
Suda T
Nagata S
Article Info
Journal
International immunology
Abbr.
Int Immunol
ISSN
0953-8178
Published
1994-10-00
Pages
1567-74
Language
English
Region
England
NLM ID
8916182
Subset
IM
Databases
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